Guest guest Posted June 29, 2007 Report Share Posted June 29, 2007 I have a bit of an annoyance. I joined the Auditory Processing Boad on thinking that I would hear about the things that the parents were doing and possibly offer some input. All of the parents there seem to be using 'one product' which is an extremely expensive, hard to get program called FastForward. It requires a therapist or a school systems approval to obtain. The board is moderated by an audiologist so I thought I might learn something. This one poor mom after months of fighting with the system finally got the program and tried to get her son to use it (75 minutes per day is required for success! - yikes!); he thought it was boring and refused to comply. I sent in a post advocating books on tape, digit spans, The Listening Program and any other alternatives for stimulating auditory I could think of. The moderator would not post the message. That was not the first time this has happened on that board. I realized that Auditory Processing board is being used for the purpose of 'selling' these parents this product and really not introducing them to any thing else. This really made me angry. These parents/kids should be able to get 'the best help' from many products not just being 'duped' into thinking that only one thing works for our kids. It truly makes me appreciate our board and the dyspraxia families board where all information is shared in an open, trusting and do what's best for your child, way. Thank you 'whoever moderates this board'! You have enabled 'free speech' and free sharing of ideas and created a special place where we can get our kids better using the knowledge and experience of others as our guide. I don't know who you are but you are GREAT! Janice Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2007 Report Share Posted June 29, 2007 Thanks Janice -I too believe in free speech. I'm the group owner and there are 10 moderators who have children with various diagnosis and who don't share all of my views. Nobody is perfect and all should be challenged -that includes me. Sometimes people complain to me offlist about why there isn't more talk about this or that (like therapy) and I always say that this group has a mind of it's own and if one wants to talk about something -then just post about it and see if others want to talk about it too. We all have things to teach and things to learn -that's how we grow and best help our children overcome! About the problem with that board -Dr. Tallal is one of the advisors to both CHERAB http://www.cherab.org/information/speechlanguage/phonologicalawareness activities.html and Speechville http://www.speechville.com/bios/tallal.html and she was one of the creators of FastForWord. Do you want me to share this with her and get a response you can post to this group? ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2007 Report Share Posted June 29, 2007 I don't want to create a 'stink' but I do feel sorry for those parents and their children who mistakenly believe that this program is the ONLY way to help their kids. A lot of the stuff we can do for our children is accessible to all and doesn't require spending all of your family resources. While some $$$ is useful to purchase the latest in technology, it doesn't have to be a requirement for helping your child successfully. I was indeed disappointed to find that my posts advocating other ideas and other potential solutions have mostly not made it to that board. In the end, it makes me appreciate what a special place our board is. I say it again. You have created a WONDERFUL place where I can trust that we will hear a wide variety of viewpoints, opinions and sharing of what works for our little ones without censureship. Our children are so precious and we are all so dedicated to helping them. I have learned so much here and hopefully have taught much too. I came on to this board knowing a lot of therapy techniques but little about the importance of vitamins and resolving the 'gut' issues. It is the first place I come to for my morning coffee! So, a heartfelt THANK YOU is in order! We moms on this board have found peace and comfort in sharing our wisdom and we owe it all in great measure to you.... Janice [sPAM] [ ] Re: Off Topic - Our special 'Board' Thanks Janice -I too believe in free speech. I'm the group owner and there are 10 moderators who have children with various diagnosis and who don't share all of my views. Nobody is perfect and all should be challenged -that includes me. Sometimes people complain to me offlist about why there isn't more talk about this or that (like therapy) and I always say that this group has a mind of it's own and if one wants to talk about something -then just post about it and see if others want to talk about it too. We all have things to teach and things to learn -that's how we grow and best help our children overcome! About the problem with that board -Dr. Tallal is one of the advisors to both CHERAB http://www.cherab.org/information/speechlanguage/phonologicalawareness activities.html and Speechville http://www.speechville.com/bios/tallal.html and she was one of the creators of FastForWord. Do you want me to share this with her and get a response you can post to this group? ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2007 Report Share Posted June 29, 2007 Janice...I am on that board too and I have had a different experience. My first introduction email was answered by several people with lots of advice...mostly books to read. Also, I learned from the audiologist who moderates the board that children in preschool can be tested for APD. That was definitely of interest to me because I had always been told they had to be 6 or 7. Actually no one tried to sell me Fast Forward either. It is not anywhere near as active as this board but I have gotten answers to any questions I have asked. I definitely agree with you though about this board. It is special. ) Aggie [ ] Re: Off Topic - Our special 'Board' I have a bit of an annoyance. I joined the Auditory Processing Boad on thinking that I would hear about the things that the parents were doing and possibly offer some input. All of the parents there seem to be using 'one product' which is an extremely expensive, hard to get program called FastForward. It requires a therapist or a school systems approval to obtain. The board is moderated by an audiologist so I thought I might learn something. This one poor mom after months of fighting with the system finally got the program and tried to get her son to use it (75 minutes per day is required for success! - yikes!); he thought it was boring and refused to comply. I sent in a post advocating books on tape, digit spans, The Listening Program and any other alternatives for stimulating auditory I could think of. The moderator would not post the message. That was not the first time this has happened on that board. I realized that Auditory Processing board is being used for the purpose of 'selling' these parents this product and really not introducing them to any thing else. This really made me angry. These parents/kids should be able to get 'the best help' from many products not just being 'duped' into thinking that only one thing works for our kids. It truly makes me appreciate our board and the dyspraxia families board where all information is shared in an open, trusting and do what's best for your child, way. Thank you 'whoever moderates this board'! You have enabled 'free speech' and free sharing of ideas and created a special place where we can get our kids better using the knowledge and experience of others as our guide. I don't know who you are but you are GREAT! Janice Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2007 Report Share Posted June 29, 2007 Aggie, Just about every message I had posted informing and advocating other techniques and technologies did not made it to the board. (I put a lot of time and thought into those posts) At any rate, I'll just stick close to 'our home'. Janice [ ] Re: Off Topic - Our special 'Board' I have a bit of an annoyance. I joined the Auditory Processing Boad on thinking that I would hear about the things that the parents were doing and possibly offer some input. All of the parents there seem to be using 'one product' which is an extremely expensive, hard to get program called FastForward. It requires a therapist or a school systems approval to obtain. The board is moderated by an audiologist so I thought I might learn something. This one poor mom after months of fighting with the system finally got the program and tried to get her son to use it (75 minutes per day is required for success! - yikes!); he thought it was boring and refused to comply. I sent in a post advocating books on tape, digit spans, The Listening Program and any other alternatives for stimulating auditory I could think of. The moderator would not post the message. That was not the first time this has happened on that board. I realized that Auditory Processing board is being used for the purpose of 'selling' these parents this product and really not introducing them to any thing else. This really made me angry. These parents/kids should be able to get 'the best help' from many products not just being 'duped' into thinking that only one thing works for our kids. It truly makes me appreciate our board and the dyspraxia families board where all information is shared in an open, trusting and do what's best for your child, way. Thank you 'whoever moderates this board'! You have enabled 'free speech' and free sharing of ideas and created a special place where we can get our kids better using the knowledge and experience of others as our guide. I don't know who you are but you are GREAT! Janice Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2007 Report Share Posted June 29, 2007 Janice, Thanks for your observation I just started with one that seems to be kinda " selling products " too. I want to thank everyone on this board too- I am so appreciative of all the responses to my questions- particularly about the ABA, dosing..... . I have felt very alone with - who has no diagnosis, but I feel so much " at home " with this amazing board and it has given my husband and I such hope and encouragement to keep going!!!! Thanks to all, Kathy ________________________________________________________________________________\ ____ Building a website is a piece of cake. Small Business gives you all the tools to get online. http://smallbusiness./webhosting Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2007 Report Share Posted June 29, 2007 Just wanted to make a Fast Forward comment. An excellent sensory OT in our area said that The Therapeutic Listening program should be used before the Fast Forward program. She has seen quite a few kids not benefit from Fast Forward until she took them back to the " basics " and had them do The Therapeutic Listening program. M. > > I don't know Janet. I've only posted a few times to that board but they always posted and I was satisfied with the answers. The last time, I asked some questions about my grandson and the doctor emailed me off the board because of confidentiality reasons. I liked him a lot and I am probably going to make an appointment with him. He seems like he knows a lot about young children and APD. I am trying to figure out whether he is in network or not. I'm sorry that happened to you. This board does have a very knowledgeable group of people who are very willing to share. Aggie > [ ] Re: Off Topic - Our special 'Board' > > I have a bit of an annoyance. > > I joined the Auditory Processing Boad on thinking that I would hear about the things that the parents were doing and possibly offer some input. All of the parents there seem to be using 'one product' which is an extremely expensive, hard to get program called FastForward. It requires a therapist or a school systems approval to obtain. The board is moderated by an audiologist so I thought I might learn something. > > This one poor mom after months of fighting with the system finally got the program and tried to get her son to use it (75 minutes per day is required for success! - yikes!); he thought it was boring and refused to comply. > > I sent in a post advocating books on tape, digit spans, The Listening Program and any other alternatives for stimulating auditory I could think of. > > The moderator would not post the message. That was not the first time this has happened on that board. I realized that Auditory Processing board is being used for the purpose of 'selling' these parents this product and really not introducing them to any thing else. > > This really made me angry. These parents/kids should be able to get 'the best help' from many products not just being 'duped' into thinking that only one thing works for our kids. > > It truly makes me appreciate our board and the dyspraxia families board where all information is shared in an open, trusting and do what's best for your child, way. > > Thank you 'whoever moderates this board'! You have enabled 'free speech' and free sharing of ideas and created a special place where we can get our kids better using the knowledge and experience of others as our guide. I don't know who you are but you are GREAT! > > Janice > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 30, 2007 Report Share Posted June 30, 2007 We also looked into Fast Forword at one point. I talked with a therapist who administers the program and posted on another special needs board to get advice. The program is very expensive and all the moms who posted on the special needs board said it did help some but felt for the money it wasn't really worth it. Thankfully we have seen much progress with other, more affordable solutions, many of which have been recommended here. Add my " thanks " to all the others, both for the board and for all the dedicated moms out there willing to share what they have learned. You ladies are awesome! Kim with 4 cuties elmccann <elmccann@...> wrote: Just wanted to make a Fast Forward comment. An excellent sensory OT in our area said that The Therapeutic Listening program should be used before the Fast Forward program. She has seen quite a few kids not benefit from Fast Forward until she took them back to the " basics " and had them do The Therapeutic Listening program. M. > > I don't know Janet. I've only posted a few times to that board but they always posted and I was satisfied with the answers. The last time, I asked some questions about my grandson and the doctor emailed me off the board because of confidentiality reasons. I liked him a lot and I am probably going to make an appointment with him. He seems like he knows a lot about young children and APD. I am trying to figure out whether he is in network or not. I'm sorry that happened to you. This board does have a very knowledgeable group of people who are very willing to share. Aggie > [ ] Re: Off Topic - Our special 'Board' > > I have a bit of an annoyance. > > I joined the Auditory Processing Boad on thinking that I would hear about the things that the parents were doing and possibly offer some input. All of the parents there seem to be using 'one product' which is an extremely expensive, hard to get program called FastForward. It requires a therapist or a school systems approval to obtain. The board is moderated by an audiologist so I thought I might learn something. > > This one poor mom after months of fighting with the system finally got the program and tried to get her son to use it (75 minutes per day is required for success! - yikes!); he thought it was boring and refused to comply. > > I sent in a post advocating books on tape, digit spans, The Listening Program and any other alternatives for stimulating auditory I could think of. > > The moderator would not post the message. That was not the first time this has happened on that board. I realized that Auditory Processing board is being used for the purpose of 'selling' these parents this product and really not introducing them to any thing else. > > This really made me angry. These parents/kids should be able to get 'the best help' from many products not just being 'duped' into thinking that only one thing works for our kids. > > It truly makes me appreciate our board and the dyspraxia families board where all information is shared in an open, trusting and do what's best for your child, way. > > Thank you 'whoever moderates this board'! You have enabled 'free speech' and free sharing of ideas and created a special place where we can get our kids better using the knowledge and experience of others as our guide. I don't know who you are but you are GREAT! > > Janice > > Quote Link to comment Share on other sites More sharing options...
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